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Metadata
ID	DOID:0080516
Name	Meier-Gorlin syndrome 5
Definition	A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CDC6 gene on chromosome 17q21. https://pubmed.ncbi.nlm.nih.gov/11477602/
Xrefs	MIM:613805
Parent Relationships	is_a Meier-Gorlin syndrome is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance